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Muscular Dystrophy, Duchenne
Known as:
Cardiomyopathy, Dilated, X-Linked
, x-linked muscular dystrophy
, Pseudohypertrophic Childhood Muscular Dystrophy
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An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the…
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National Institutes of Health
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Related topics
Related topics
23 relations
Becker Muscular Dystrophy
Cardiomyopathy, Dilated
Congestive heart failure
Connective and Soft Tissue
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Broader (2)
Duchenne and Becker Muscular Dystrophy
Muscular Dystrophy
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2016
Highly Cited
2016
In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy
Christopher E Nelson
,
Chady H Hakim
,
+11 authors
C. Gersbach
Science
2016
Corpus ID: 206643555
Editing can help build stronger muscles Much of the controversy surrounding the gene-editing technology called CRISPR/Cas9…
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Highly Cited
2011
Highly Cited
2011
American College of Sports Medicine position stand. Quantity and quality of exercise for developing and maintaining cardiorespiratory, musculoskeletal, and neuromotor fitness in apparently healthy…
C. Garber
,
B. Blissmer
,
+5 authors
D. Swain
Medicine & Science in Sports & Exercise
2011
Corpus ID: 3548491
The purpose of this Position Stand is to provide guidance to professionals who counsel and prescribe individualized exercise to…
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Highly Cited
2011
Highly Cited
2011
Systemic administration of PRO051 in Duchenne's muscular dystrophy.
N. Goemans
,
M. Tulinius
,
+16 authors
J. V. van Deutekom
New England Journal of Medicine
2011
Corpus ID: 9877191
BACKGROUND Local intramuscular administration of the antisense oligonucleotide PRO051 in patients with Duchenne's muscular…
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Review
2010
Review
2010
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management
K. Bushby
,
R. Finkel
,
+11 authors
C. Constantin
Lancet Neurology
2010
Corpus ID: 328499
Highly Cited
1991
Highly Cited
1991
The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy
H. Stedman
,
H. Sweeney
,
+7 authors
A. Kelly
Nature
1991
Corpus ID: 4302451
ALTHOUGH murine X-linked muscular dystrophy (mdx) and Duchenne muscular dystrophy (DMD) are genetically homologous and both…
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Highly Cited
1989
Highly Cited
1989
The molecular basis of muscular dystrophy in the mdx mouse: a point mutation.
P. Sicinski
,
Y. Geng
,
A. S. Ryder-Cook
,
E. Barnard
,
M. Darlison
,
P. J. Barnard
Science
1989
Corpus ID: 39661171
The mdx mouse is an X-linked myopathic mutant, an animal model for human Duchenne muscular dystrophy. In both mouse and man the…
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Highly Cited
1988
Highly Cited
1988
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification.
J. Chamberlain
,
R. Gibbs
,
J. Ranier
,
P. Nguyen
,
C. Caskey
Nucleic Acids Research
1988
Corpus ID: 24671501
The application of recombinant DNA technology to prenatal diagnosis of many recessively inherited X-linked diseases is…
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Highly Cited
1988
Highly Cited
1988
Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy.
E. Hoffman
,
K. Fischbeck
,
+7 authors
L. Specht
New England Journal of Medicine
1988
Corpus ID: 27471444
A deficiency of the protein dystrophin has recently been shown to be the probable cause of Duchenne's muscular dystrophy. We…
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Highly Cited
1987
Highly Cited
1987
Dystrophin: The protein product of the duchenne muscular dystrophy locus
E. Hoffman
,
Robert H. Brown
,
L. Kunkel
Cell
1987
Corpus ID: 33548364
Highly Cited
1987
Highly Cited
1987
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
M. Koenig
,
E. Hoffman
,
C. Bertelson
,
A. Monaco
,
C. Feener
,
L. Kunkel
Cell
1987
Corpus ID: 35668717
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